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A Thematic Analysis of Compassion Rounds

5 maggio 2021 aggiornato da: AdventHealth

A Thematic Analysis of the Effects of Compassion Rounds on Clinicians and the Families of NICU Patients

The primary objective of this thematic analysis is to understand the experience of "Compassion Rounds" for patients, families, friends, and clinicians. The secondary objective of this study is to evaluate and interpret data to determine best practice recommendations for standardization and scalability.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

This research will be conducted as a Thematic Analysis. Participants will be recruited from those who take part in compassion rounds, including patients, their loved ones, physicians, chaplains, social workers, nurses, and other care providers.

Qualitative data on participants' experiences throughout the intervention will be collected and analyzed using thematic methodology. The data will be used to explain the psychosocial processes that influence participant experience and reported outcomes.

Qualitative methodology does not seek to verify hypotheses based on logical assumptions, as quantitative measures do, instead it is used to derive salient constructs directly from the data. This methodology allows inductive understanding of participants' social reality and perceptions of the treatment, resulting in explanations of how the treatment leads to outcomes and the identification of variables that may then be quantified for more generalizable study.

Semi-structured Interviews

Through semi-structured interviews, which will be recorded and transcribed, the researcher asks participants open-ended questions intended to elicit perspectives on their experience of compassion rounds, without limiting responses to pre-determined categories of interest. The following are examples:

"What/who do you remember most vividly?" "How would you describe your experience to a friend?" "What was most meaningful to you? "What made you feel uncomfortable?" "Would you do it again? Why or why not?" "What, if anything, changed after compassion rounding?"

Coding

The researcher codes and documents throughout data collection and analysis to lend transparency to the coding process and to keep a record of ideas to inform thematic exposition. The researcher assigns categorical codes (labels or concepts) to the transcribed responses line-by-line, analyzing patterns of relationships and using a constant comparison technique to identify similarities and differences throughout the data. The following coding techniques will be used to analyze transcriptions:

  • open coding: the researcher segments the data into preliminary categories, based on similarity
  • axial coding: the researcher groups the categories into themes that provide new ways of seeing and understanding the phenomenon under study
  • selective coding: the researcher integrates the categories and themes to articulate a coherent theory of the phenomenon of study.

Theoretical Sampling Grounded theory research uses "theoretical sampling" to identify participants for interviews. Purposive samples are identified to initiate data collection and analysis, and to select participants who are likely to clarify, verify, or contradict data as it is collected. Sampling concludes when the data is "saturated," which occurs when coded categories are well-defined and no new significant insights are emerging from interviews.

Thematic Development and Validation

The researcher develops thematic explanations that stem from rendering participants' experiences throughout the practice of compassion rounding.

Themes are evaluated for fit and relevance and employee participants may be asked to validate the researcher's findings in follow-up interviews and focus groups.

Observation The researcher will also observe compassion rounding to collect data that will provide further insight to participants' experiences. Observations of interactions and reactions in real time will be documented and the data will be coded and analyzed using the techniques described above. Observational data will not be integrated into interview data, but will be used to confirm or contrast reported data.

Tipo di studio

Osservativo

Iscrizione (Effettivo)

30

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Florida
      • Orlando, Florida, Stati Uniti, 32804
        • AdventHealth Orlando

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Participants will be recruited from participants in compassion rounding, including patients, their loved ones, physicians, chaplains, social workers, nurses, and other care providers.

Descrizione

Inclusion Criteria:

  1. An employee of Florida Hospital or Adventist Health System, or a physician with privileges there, or a patient, or a family or friend who has participated in compassion rounding at a Florida Hospital critical care unit
  2. Over the age of 18
  3. Able to provide informed consent
  4. Must speak and understand English
  5. Willing and able to provide a contact phone number

Exclusion Criteria:

1. Discernible cognitive impairment

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Physicians
interview physicians who have conducted compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Chaplains
interview chaplains who have conducted compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Other Healthcare Providers
interview other healthcare providers who have conducted compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Patients
interview patients who have participated in compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Patient family members/friends
interview patient's loved ones who have participated with the patient in compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Validated Thematic Framework to Explain the Effects of Compassion Rounding
Lasso di tempo: five months
Analysis of data collected throughout the study will result in a validated theoretical framework to understand and explain the psychosocial processes that influence participant experience and reported outcomes.
five months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Compendium of Evidence-Based Best Practices for the Implementation of Compassion Rounding
Lasso di tempo: five months
Analysis of data collected throughout the study will result in an evidence-based compendium of best practices for the implementation of compassion rounding.
five months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Kim McManus, Ph.D., FH Center for CREATION Health Research

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 ottobre 2018

Completamento primario (Effettivo)

31 luglio 2019

Completamento dello studio (Effettivo)

28 agosto 2019

Date di iscrizione allo studio

Primo inviato

15 agosto 2018

Primo inviato che soddisfa i criteri di controllo qualità

23 agosto 2018

Primo Inserito (Effettivo)

28 agosto 2018

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 maggio 2021

Ultimo aggiornamento inviato che soddisfa i criteri QC

5 maggio 2021

Ultimo verificato

1 maggio 2021

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 1320386

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su interview

3
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